Evidence map›Paper›PMID 30363449›Full record

ArticleMovement disorders clinical practice

Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression.

Alhassane Diallo, Heike Jacobi, Tanja Schmitz-Hübsch, Arron Cook, Robyn Labrum, Alexandra Durr, Alexis Brice, Perrine Charles, Cecilia Marelli, Caterina Mariotti and 24 more

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Article in Movement disorders clinical practice. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

34 authors at 20 institutions in 10 countries.

Alhassane DialloParis-Sorbonne Universités Université Pierre et Marie Curie UMR 1136 Institut National de la Santé et de la Recherche Médicale (INSERM) Institut Pierre Louis d'Epidémiologie et de Santé Publique Paris France.
Heike JacobiDepartment of Neurology University Hospital of Bonn Bonn Germany.
Tanja Schmitz-HübschClinical Neuroimmunology Groupe NeuroCure Clinical Research Center Charité Universitätsmedizin Berlin Berlin Germany.
Arron CookDepartment of Molecular Neuroscience Institute of Neurology University College London London United Kingdom.ORCID 0000-0002-1261-9068
Robyn LabrumNeurogenetic Laboratory National Hospital of Neurology and Neurosurgery University College London Hospitals London United Kingdom.
Alexandra DurrParis-Sorbonne Universités Université Pierre et Marie Curie UMR S1127 INSERM Paris France.
Alexis BriceParis-Sorbonne Universités Université Pierre et Marie Curie UMR S1127 INSERM Paris France.
Perrine CharlesGenetic Department Pitié-Salpêtrière University Hospital Assistance Publique-Hôpitaux de Paris Paris France.
Cecilia MarelliService de Neurologie Centre Mémoire de Resources et de Recherche Hôpital Gui de Chauliac Montpellier France.
Caterina MariottiSOSD Genetics of Neurodegenerative and Metabolic Diseases Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Milan Italy.
Lorenzo NanettiSOSD Genetics of Neurodegenerative and Metabolic Diseases Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Milan Italy.
Marta PanzeriSOSD Genetics of Neurodegenerative and Metabolic Diseases Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Milan Italy.
Maria RakowiczDepartment of Clinical Neurophysiology Institute of Psychiatry and Neurology Warsaw Poland.
Anna SobanskaDepartment of Clinical Neurophysiology Institute of Psychiatry and Neurology Warsaw Poland.
Anna SulekDepartment of Genetics Institute of Psychiatry and Neurology Warsaw Poland.
Ludger SchölsDepartment of Neurodegeneration and Hertie Institute for Clinical Brain Research University of Tübingen and Deutsches Zentrum für Neurodegenerative Erkrankungen Tübingen Germany.
Holger HengelDepartment of Neurodegeneration and Hertie Institute for Clinical Brain Research University of Tübingen and Deutsches Zentrum für Neurodegenerative Erkrankungen Tübingen Germany.
Bela MeleghDepartment of Medical Genetics and Szentagothai Research Center University of Pécs Pécs Hungary.
Alessandro FillaDepartment of Neuroscience and Reproductive and Odontostomatological Sciences Federico II University Naples Italy.
Antonella AntenoraDepartment of Neuroscience and Reproductive and Odontostomatological Sciences Federico II University Naples Italy.
Jon InfanteNeurology Service University Hospital Marqués de Valdecilla University of Cantabria and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED) Santander Spain.
José BercianoNeurology Service University Hospital Marqués de Valdecilla University of Cantabria and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED) Santander Spain.
Bart P van de WarrenburgDepartment of Neurology Donders Institute for Brain, Cognition and Behavior Radboud University Medical Center Nijmegen the Netherlands.
Dagmar TimmannDepartment of Neurology University Clinic Essen University of Duisburg-Essen Duisburg Germany.
Sylvia BoeschDepartment of Neurology Medical University Innsbruck Innsbruck Austria.
Massimo PandolfoNeurology Service Laboratory of Experimental Neurology Université Libre de Bruxelles Hôpital Erasme Brussels Belgium.
Jörg B SchulzDepartment of Neurology Rheinisch-Westfälische Technische Hochschule Aachen University Aachen Germany.
Peter BauerInstitute of Medical Genetics and Applied Genomics University of Tübingen Tübingen Germany.
Paola GiuntiDepartment of Molecular Neuroscience Institute of Neurology University College London London United Kingdom.
Laszlo BalikoDepartment of Neurology Zala County Hospital Zalaegerszeg Hungary.
Michael H ParkinsonDepartment of Molecular Neuroscience Institute of Neurology University College London London United Kingdom.
Jun-Suk KangDepartment of Neurology University of Frankfurt Frankfurt am Main Germany.
Thomas KlockgetherDepartment of Neurology and German Center for Neurodegenerative Diseases University Hospital of Bonn Bonn Germany.
Sophie Tezenas du MontcelParis-Sorbonne Universités Université Pierre et Marie Curie UMR 1136 Institut National de la Santé et de la Recherche Médicale (INSERM) Institut Pierre Louis d'Epidémiologie et de Santé Publique Paris France.
Inserm · FRGerman Center for Neurodegenerative Diseases · DEInstitute of Psychiatry and Neurology · PLIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity College London · GBFederico II University Hospital · ITUniversidad de Cantabria · ESCharité - Universitätsmedizin Berlin · DEGoethe University Frankfurt · DEHeidelberg University · DEHôpital Gui de Chauliac · FRInnsbruck Medical University · ATJülich Aachen Research Alliance · DERadboud University Nijmegen · NLRoyal London Hospital · GBSorbonne Université · FRUniversité Libre de Bruxelles · BEUniversity of Duisburg-Essen · DEUniversity of Pecs · HUUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpinocerebellar ataxias (SCAs) are dominantly inherited, progressive ataxia disorders. Disease progression could be preceded by weight loss.

objectivesWe aimed to study the course of weight loss in patients who had the most common SCAs (SCA1, SCA2 SCA3, and SCA6). Additional objectives were to identify subgroups of weight evolution, to determine the factors influencing these evolutions, and to assess the impact of these evolutions on disease progression.

methodsIn total, 384 patients from the EUROSCA prospective cohort study were analyzed who had SCA1, SCA2, SCA3, or SCA6 and at least 3 measurements of weight. Age was used as a time scale. Clinical outcomes were body mass index (BMI) and the Scale for the Assessment and Rating Ataxia (SARA), with scores ranging from 0 to 40. We used a linear mixed model to analyze the course of BMI and a latent class mixed model to identify subgroup BMI evolution.

resultsOverall, BMI declined over time (-0.11 ± 0.03 kg/m

conclusionsThe current data have substantial implications for the design of future interventional studies in SCA, as they provide a basis for patient stratification and emphasize the usefulness of BMI as a biomarker for monitoring disease progression.

Indexed as

body mass indexlatent class mixed modellongitudinal dataspinocerebellar ataxia

Identifiers

PMID30363449
PMCPMC6174467
OpenAlexW2736736667

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.